Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
R124 reovirus is an experimental oncolytic mammalian orthoreovirus (MRV) derived from the Type 3 Dearing (T3D) strain. It is specifically engineered with a point mutation in the S1 gene segment, resulting in a proline-to-serine substitution at residue 124 (P124S) of the sigma 1 (σ1) attachment protein. This modification enables the virus to infect cells via a Junctional Adhesion Molecule-A (JAM-A)-independent pathway, likely by utilizing alternative receptors such as sialic acid. This expanded tropism allows R124 to target cancer cells that have downregulated JAM-A, a common mechanism of resistance to wild-type reovirus infection. Developed at Leiden University Medical Center (LUMC), R124 serves as a prototype for JAM-A independent (jin) mutants and has demonstrated preclinical efficacy in various tumor models, including prostate cancer and glioblastoma, by inducing direct oncolysis and stimulating anti-tumor immune responses.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on R124 reovirus.